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464401 to 464500 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Prevalence of dens invaginatus in Jordanian adults.
Nonrecognition and subsequent endodontic treatment of dens invaginatus.
Dens invaginatus in the maxillary lateral incisor: treatment of 3 cases.
Anatomical redesign for the treatment of dens invaginatus type III with open apexes: a literature review and case presentation.
A previously unreported association between Nance-Horan syndrome and spontaneous dental abscesses.
Mineral trioxide aggregate obturation: a review and case series.
Characteristics of incisor-premolar hypodontia in families.
A rare presentation of dens invaginatus in a mandibular lateral incisor occurring concurrently with bilateral maxillary dens invaginatus: case report and review of literature.
Dens invaginatus. Part 1: classification, prevalence and aetiology.
Biologically based treatment of immature permanent teeth with pulpal necrosis: a case series.
Dens invaginatus: aetiology, classification, prevalence, diagnosis, and treatment considerations.
Dens invaginatus (dilated composite odontome). I. Variations of the invagination process and associated anterior crown forms.
Progressive, generalized, apical idiopathic root resorption and hypercementosis.
Hypercementosis--an important clue to Paget disease of the maxilla.
Finite element analysis of equine incisor teeth. Part 2: investigation of stresses and strain energy densities in the periodontal ligament and surrounding bone during tooth movement.
Equine odontoclastic tooth resorption and hypercementosis.
Enlarged occlusal surfaces on first molars due to severe attrition and hypercementosis: examples from prehistoric coastal populations of Texas.
Enamel dysplasia with hamartomatous atypical follicular hyperplasia: review of the literature and report of a case.
Enamel dysplasia with hamartomatous atypical follicular hyperplasia (EDHFH) syndrome: suggested pathogenic mechanisms.
Early Pleistocene human mandible from Sima del Elefante (TE) cave site in Sierra de Atapuerca (Spain): a palaeopathological study.
Dental patient with acromegaly: a case report.
A contribution to the histological study of hypercementosis using metal staining.
Secondary retention of permanent molars: a histologic study.
Guanylin and functional coupling proteins in the human salivary glands and gland tumors : expression, cellular localization, and target membrane domains.
Osteomyelitis of the mandible associated with autosomal dominant osteopetrosis: a case report.
Cytogenetic analysis of salivary gland type tumors.
Implications of tooth root hypercementosis in a Barbados slave skeletal collection.
Identification of oncocytic lesions of salivary glands by anti-mitochondrial immunohistochemistry.
Effect of HIP/ribosomal protein L29 deficiency on mineral properties of murine bones and teeth.
Clinical analysis of salivary gland tumor cases in West China in past 50 years.
Alveolar bone loss of senescence-accelerated mouse (SAM).
Salivary gland tumors in a Brazilian population: a retrospective study of 124 cases.
A scanning electron microscopic study of hypercementosis.
Studies of dental root surface caries. 2: The role of cementum in root surface caries.
Cemento-osseous dysplasia of the jaws in 54 Japanese patients: a radiographic study.
Parotid gland tumors: can addition of diffusion-weighted MR imaging to dynamic contrast-enhanced MR imaging improve diagnostic accuracy in characterization?
Histogenic classification of salivary tumors.
Differentiation of benign and malignant parotid tumors using deconvolution-based perfusion CT imaging: feasibility of the method and initial results.
Immunolocalization of matrix metalloproteinases-2 and -9 during apical periodontitis development.
Histogenesis of papillary cystadenoma lymphomatosum (Warthin's tumor) of the parotid salivary gland.
Benign and malignant oncocytoma.
A study of MECT1-MAML2 in mucoepidermoid carcinoma and Warthin's tumor of salivary glands.
Fine-needle aspiration cytology of salivary gland: a review of 341 cases.
Recoverin-associated retinopathy: a clinically and immunologically distinctive disease.
Detection of damage to the mitochondrial genome in the oncocytic cells of Warthin's tumour.
CRTC1/MAML2 fusion transcript in high grade mucoepidermoid carcinomas of salivary and thyroid glands and Warthin's tumors: implications for histogenesis and biologic behavior.
Altered Notch signaling resulting from expression of a WAMTP1-MAML2 gene fusion in mucoepidermoid carcinomas and benign Warthin's tumors.
A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type I.
Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletion.
New perspectives on the molecular basis of hereditary bone tumours.
Constipation, Episodic Scotomas, Low Self-Esteem
Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome.
Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and III.
Clinical and molecular characterization of a patient with Langer-Giedion syndrome and mosaic del(8)(q22.3q24.13).
A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1).
Missense mutation of TRPS1 in a family of tricho-rhino-phalangeal syndrome type III.
Further case of microdeletion of 8q24 with phenotype overlapping Langer-Giedion without TRPS1 deletion.
Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes.
Classification of osteogenesis imperfecta by dental characteristics.
Construction and characterization of band-specific DNA libraries.
Genetic evidence for key roles of decorin and biglycan in dentin mineralization.
Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.
Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II.
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome.
Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II.
Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome.
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11.
Chest Pain, Rectal Bleeding, Volvulus, chest pain worse on breathing, diarrhea, dyschezia, blood in stool, acute diarrhea, abdominal pain, flatulence, pyrosis, chest pain rectal bleeding constipation and dirreah headaches depression
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.
Hereditary multiple exostoses.
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I.
The carboxyl-terminal domain of phosphophoryn contains unique extended triplet amino acid repeat sequences forming ordered carboxyl-phosphate interaction ridges that may be essential in the biomineralization process.
The importance of intrafibrillar mineralization of collagen on the mechanical properties of dentin.
The gene associated with trichorhinophalangeal syndrome in humans is overexpressed in breast cancer.
A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.
DSPP mutation in dentinogenesis imperfecta Shields type II.
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.
Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III.
Metastatic and histologic presentations in unknown primary cancer.
Low values of 5-hydroxymethylcytosine (5hmC), the "sixth base," are associated with anaplasia in human brain tumors.
Loss of p53 promotes anaplasia and local invasion in ret/PTC1-induced thyroid carcinomas.
Gangliogliomas: an intriguing tumor entity associated with focal epilepsies.
Structural and functional changes of normal aging skin.
Smooth muscle tumors of the gastrointestinal tract. What we know now that Stout didn't know.
Anaplastic large cell Ki-1 lymphoma. Delineation of two morphological types.
The TP53-ARF tumor suppressor pathway is frequently disrupted in large/cell anaplastic medulloblastoma.
Gliomas: classification with MR imaging.
Comparative genomic hybridization detects an increased number of chromosomal alterations in large cell/anaplastic medulloblastomas.
Skin diseases in south-east Nigeria: a current perspective.
c-myc overexpression causes anaplasia in medulloblastoma.
Depression and suicidal behavior in acne patients treated with isotretinoin: a systematic review.
Histopathological and molecular prognostic markers in medulloblastoma: c-myc, N-myc, TrkC, and anaplasia.
Acquired trichomegaly and symptomatic external ocular changes in patients receiving epidermal growth factor receptor inhibitors: case reports and a review of literature.
Histopathologic grading of medulloblastomas: a Pediatric Oncology Group study.
Histopathology and prognosis of Wilms tumors: results from the First National Wilms' Tumor Study.